22328-44-5

Upstream product

• 42006-91-7 4-bromobenzyl-α,α-d₂ alcohol 
• 78585-64-5 1-bromo-4-(bromo di-deuteromethyl)benzene 
• 1124-18-1 toluene-d3 
• 865-50-9 iodomethane-d3 
• 106-37-6 1.4-dibromobenzene 
• 619-42-1 4-methoxycarbonylphenyl bromide 

Downstream Products

• 95249-73-3 C₁₅H₁₂⁽²⁾H₃BrO 
• 131088-99-8 α,α,α-<2H3>p-tolunitrile 
• 19315-35-6 ethyl 4-methyl-d3-benzoate 
• 95249-78-8 C₁₈H₁₇⁽²⁾H₃O 
• 95249-74-4 C₂₁H₁₆⁽²⁾H₃BrS 
• 95249-76-6 C₁₈H₁₆⁽²⁾H₃BrO 
• 78585-67-8 4-methyl-d3-benzyl alcohol 
• 114563-29-0 4-methyl-d3-benzyl bromide 

Relevant academic research and scientific papers

NOVEL ORGANIC COMPOUND AND MATERIALS FOR ORGANIC ELECTROLUMINESCENT DEVICES COMPRISING THE SAME AND ORGANIC ELECTROLUMINESCENT DEVICES COMPRISING THE SAME

The present invention provides a novel organic compound represented by chemical formula 1, a material for an organic electroluminescent device including the organic compound, and an organic electroluminescent device. The present invention can improve thermal stability, color purity, and device life.

AMINOPYRAZINE DIOL COMPOUNDS AS PI3K-y INHIBITORS

This application relates to compounds of Formula (I): or pharmaceutically acceptable salts thereof, which are inhibitors of PI3K-γ which are useful for the treatment of disorders such as autoimmune diseases, cancer, cardiovascular diseases, and neurodegenerative diseases.

Synthesis of Isotopically Labeled Tri-p-tolylamine

Three isotopically labeled tri-p-tolylamines, 15N, 15N2D2, and mono-13CH3, have been prepared using zeolite mediated bromination or nitration of toluenes as one of the key steps. The obtained 4-nitrotoluenes were reduced to 4-aminotoluenes, and coupled, v

Side Chain Hydroxylation of Aromatic Compounds by Fungi. Part 4. Influence of the para Substituent on Kinetic Isotope Effects During Benzylic Hydroxylation by Mortierella isabellina

The benzylic hydroxylation of a series of para-substituted toluenes by the fungus Mortierella isabellina has been studied by using CD3, CHD2, and CH2D methyl labelled substrates.Inter- and intramolecular primary and secondary deuterium kinetic isotope effect ratios have been determined: the intermolecular primary effects are maximal with strongly electron-withdrawing para substituents (R = CN and CF3), while the intramolecular primary effects are minimal for R = H but increase in instances where R is electron donating or withdrawing.These results are interpreted in terms of a dependence of the hydroxylation mechanism on the nature of the para substituent.

Asymmetric Synthesis. Mechanism of Asymmetric Catalytic Allylation

The mechanism of palladium-assisted asymmetric catalytic allylation has been investigated.It is found that the process involves two primary steps: the oxidative addition of a palladium(0)-phosphine species with an allyl acetate to form diastereomeric ?-al

Determination of the Heats of Formation of the Isomeric Xylylenes by Ion Cyclotron Double-Resonance Spectroscopy

Heats of formation of 50 and 53 kcal mol -1 have been measured for p- and o-xylylene by using pulsed-ion cyclotron double-resonance spectroscopy.In addition a lower bound of 76 kcal mol-1 has been obtained for the heat of formation o